Prescription stimulant prescribing, nonmedical use, and shortages: US FDA research and response

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Abstract

Shortages of prescription stimulant medications have been a challenge for patients with attention-deficit/hyperactivity disorder (ADHD) and other conditions since they began in October 2022. The US Food and Drug Administration (FDA) is committed to understanding and addressing these shortages, which are occurring in the context of significant growth in the dispensing of prescription stimulant medications to adults. Prescription stimulants are Schedule II controlled substances, defined as drugs with “high potential for abuse that may lead to severe psychological or physical dependence.” Questions remain about what is driving increased prescribing of these medications and their potential for misuse; the 2023 National Survey on Drug Use and Health estimated that 3.9 million persons aged 12 years and older in the United States used prescription stimulants nonmedically in the past year. Because the production of Schedule II substances is limited by the Drug Enforcement Administration (DEA), the usual dynamics of supply and demand in the medication marketplace do not apply.

处方兴奋剂处方、非医疗使用和短缺:美国食品和药物管理局的研究与对策
自2022年10月以来,处方兴奋剂药物的短缺一直是注意力缺陷/多动障碍(ADHD)和其他疾病患者面临的挑战。美国食品和药物管理局(FDA)致力于了解和解决这些短缺问题,这些短缺是在向成人分发处方兴奋剂药物显着增长的背景下发生的。处方兴奋剂属于附表II管制物质,定义为“滥用可能性高,可能导致严重的心理或身体依赖”的药物。是什么导致这些药物的处方增加,以及它们可能被滥用,这些问题仍然存在;2023年全国药物使用和健康调查估计,去年美国有390万12岁及以上的人非医疗性地使用处方兴奋剂。由于附表II物质的生产受到美国缉毒局(DEA)的限制,药物市场中通常的供需动态不适用。
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